Clinical trials: Documentation
Vitamin D Insufficiency, Vitamin D Deficiency
Vitamin D Inadequacy in Rural Populations, Evaluation of Correction by Food Supplementation
The purpose of the research is to describe vitamin D levels and bone status in a rural Wisconsin population. It is probable that individuals of varying age and ethnicity require different amounts of D to achieve optimal status.
- Trial name
- NCT00690417
- Testing
- Cholecalciferol (vitamin D3)
- Where
- United States
- Volunteers
- 108 people, healthy volunteers welcome
- Sponsor
- University of Wisconsin, Madison
Partial Edentulism
Long-term Performance of SLActive Implants After Immediate or Early Loading
This is a follow-up study with patients, who participated in the Straumann clinical study CR06/03. The objective is the assessment of long-term data (8 and 10 years after implantation) on the performance of immediate and early…
- Trial name
- NCT02703168
- Volunteers
- 66 people
- Sponsor
- Institut Straumann AG
Hospitalizations
The Accuracy and Efficacy of Large Language Model Written Hospital Course Summaries
Background: Physicians worldwide face an increasing administrative burden that diverts time from direct patient care. Among inpatient documentation tasks, authoring hospital course summaries is particularly time-consuming and…
- Trial name
- CLEAN (NCT07491068)
- Testing
- LLM assisted workflow for generating the hospital course summary
- Where
- Slovakia
- Volunteers
- 786 people
- Sponsor
- Pavol Jozef Safarik University
Shoulder Pain, Shoulder Impingement
Assessment of Shoulder Rehabilitation Practices and Documentation Protocols at Riphah Rehabilitation Center
This study aims to evaluate Riphah Rehabilitation Center's shoulder rehabilitation procedures and documentation guidelines. The study will specifically assess the efficacy of shoulder rehabilitation procedures, their methodology…
- Conditions
- Shoulder Pain, Shoulder Impingement, Rotator Cuff Injury
- Trial name
- NCT06773442
- Testing
- Rehabilitation Practices Group, Documentation Protocols Group
- Where
- 2 sites in Pakistan
- Volunteers
- 20 people
- Sponsor
- Riphah International University
Effectiveness of AI-assisted Clinical Documentation Tool, Healthy
Effectiveness of AI-Assisted Clinical Documentation
Effectiveness of AI-assisted clinical documentation tool (AI scribes) in healthcare services using staggered difference-in-differences and multiple sources of data including registers, questionnaires and interviews.
- Trial name
- NCT07742618
- Testing
- AI clinical documentation tool
- Where
- Finland
- Volunteers
- 400 people, healthy volunteers welcome
- Sponsor
- University of Turku
Asthma, Bronchial
REACT - REAl Care for AsThma - A Disease Study to Identify Patients With Severe Uncontrolled Asthma
This is a multi-center, single-country, single-arm, prospective, disease study to collect real world data of patients with severe uncontrolled asthma in Germany.
- Trial name
- REACT-Asthma (NCT06299306)
- Where
- 6 sites in Germany
- Volunteers
- 19 people
- Sponsor
- AstraZeneca
Multiple Sclerosis
Long Term Safety of Teriflunomide When Added to Interferon-Beta or Glatiramer Acetate in Patients With Multiple Sclerosis
The primary objective was to evaluate the long-term safety and tolerability of teriflunomide when added to treatment with interferon-β [IFN-β] or glatiramer Acetate [GA] in patients with multiple sclerosis [MS] with relapses.
- Trial name
- NCT00811395
- Testing
- Teriflunomide, Interferon-β [IFN-β], Glatiramer Acetate [GA]
- Where
- 7 sites in United States, Austria and 5 more
- Volunteers
- 182 people
- Sponsor
- Sanofi
Airway Management, Intubation; Difficult or Failed
Data-driven Development of a Core Dataset for Difficult Airway Alerts
Previous difficult airway management is the most accurate predictor of future difficulty. Consistent documentation is paramount for future airway planning, but requires reliable, reproducible and easily accessible information.
- Conditions
- Airway Management, Intubation; Difficult or Failed, Airway Complication of Anesthesia
- Trial name
- FingAIRprint (NCT07275567)
- Where
- Germany
- Volunteers
- 1,785 people
- Sponsor
- Universitätsklinikum Hamburg-Eppendorf
Burnout, Professionals, Medical Records Systems, Computerized
Ambient AI Scribe (Voa Health) in Outpatient Clinics: Draft Notes, Documentation Burden, and Well-Being
The goal of this randomized clinical trial is to learn whether an "ambient AI scribe" (Voa Health) can reduce documentation burden and improve physician well-being and patient experience in outpatient clinics.
- Conditions
- Burnout, Professionals, Medical Records Systems, Computerized, Physician-Patient Relations, Ambulatory Care
- Trial name
- SOAR (NCT07302906)
- Testing
- Ambient AI scribe for clinical documentation (Voa Health), Usual documentation without AI scribe (standard care)
- Where
- Brazil
- Volunteers
- 300 people
- Sponsor
- Pedro Angelo Basei de Paula
Ankylosing Spondylitis
Basic Documentation of Adalimumab (Humira) in Patients With Ankylosing Spondylitis (AS)
The research question explored in this study was whether the effectiveness and safety of adalimumab in participants with ankylosing spondylitis was maintained during long-term therapy in routine clinical practice in Germany.
- Trial name
- NCT01079182
- Volunteers
- 4,681 people
- Sponsor
- AbbVie (prior sponsor, Abbott)
Acromegaly
Quality of Life (QoL) in Subjects With Acromegaly Under Lanreotide Autogel® Treatment.
The purpose of the protocol is to evaluate and describe QoL, in the population of Polish acromegalic patients treated with Lanreotide Autogel® 120 mg during the 24 months (long term observation).
- Trial name
- ACRO QLQ (NCT02396966)
- Where
- 18 sites in Poland
- Volunteers
- 152 people
- Sponsor
- Ipsen
Muscle Spasticity
To Document the Effectiveness of BoNT-A Injection in Adult Subjects With Upper Limb Spasticity Following Stroke
The purpose of the study is to assess the responder rate as defined by the achievement of the primary goal from the Goal Attainment Scale following one BoNT-A injection cycle in accordance with routine practices.
- Trial name
- ULIS2 (NCT01020500)
- Where
- 96 sites in Australia, Austria and 20 more
- Volunteers
- 469 people
- Sponsor
- Ipsen
Neuraxial Anesthesia Charting
Tracking Attempts of CSE, Epidural and Spinal Insertions (TRACES)
The goal of this study is to compare observed neuraxial (Epidural, spinal, combined spinal-epidural) insertion attempts with actual documented attempts in anesthesia providers (staff, residents and fellows) at one maternal…
- Trial name
- TRACES (NCT04862611)
- Where
- Canada
- Volunteers
- 220 people, healthy volunteers welcome
- Sponsor
- University of British Columbia
Burnout
Impact of Digital Ambient EXperience on Pediatric Subspecialist Documentation Burden
This randomized quality improvement pilot project aims to assess whether the implementation of generative AI software for documentation, Microsoft Nuance's Digital Ambient eXperience (DAX) Copilot, enhances physician…
- Trial name
- NCT06812234
- Testing
- DAX Copilot
- Where
- United States
- Volunteers
- 21 people, healthy volunteers welcome
- Sponsor
- Children's Healthcare of Atlanta
Hypercholesterolemia
Safety, Tolerability, and Effect of Alirocumab in High Cardiovascular Risk Patients With Severe Hypercholesterolemia Not Adequately Controlled With Conventional Lipid-modifying Therapies (ODYSSEY APPRISE)
Primary Objective: To provide participants with severe hypercholesterolemia at risk for subsequent cardiovascular (CV) events and not adequately controlled with currently available lipid-modifying therapy (LMT) access to…
- Trial name
- NCT02476006
- Testing
- ALIROCUMAB SAR236553 (REGN727), ezetimibe, atorvastatin
- Where
- 153 sites in Austria, Belgium and 14 more
- Volunteers
- 998 people
- Sponsor
- Sanofi
Musculoskeletal Disease, Orthopedic Patients
Original Medical Notes Versus AI Plain-Language Summaries
The goal of this clinical trial is to learn how patients feel when reading their medical notes. The study compares reading the original doctor's note with reading a simpler, Artificial Intelligence (AI)-generated version written…
- Trial name
- NCT07602725
- Testing
- LLM-Generated Medical Note, Control (Original Medical Note)
- Volunteers
- 135 people
- Sponsor
- University of Texas at Austin
Beta-Thalassemia
To Document the Burden of Illness on the Quality of Life and the Impact on Healthcare Utilization in (Beta) β-thalassemia Subjects Who Are Transfusion Dependent (TD) and Non-transfusion Dependent (NTD) Receiving Standard of Care
This is a multi-site, prospective, observational study implemented in β-thalassemia treatment centers from 5 countries (Italy, Turkey, Greece, Lebanon, and Thailand).
- Trial name
- NCT02626689
- Testing
- Quality of Life (QOL) questionnaires, Healthcare Resource Utilization
- Where
- 5 sites in Greece, Italy and 3 more
- Volunteers
- 100 people
- Sponsor
- Celgene
Psoriasis
Efficacy and Safety of Topical ALT-2074 (SYI-2074) for Treatment of Chronic Plaque Psoriasis
The primary objective of this study will be to evaluate the efficacy of topical ALT-2074 applied twice daily for 28 days for treatment of chronic plaque psoriasis in adult subjects.
- Trial name
- NCT00782613
- Testing
- 4,4-dimethyl-benziso-2H-selenazine
- Where
- 3 sites in Israel
- Volunteers
- 30 people
- Sponsor
- Synvista Therapeutics, Inc
Neoplasms, Clinical Documentation
Ambient AI Documentation in Oncology Consultations
This study tests whether an artificial intelligence (AI) system can help doctors write medical notes during cancer consultations.
- Conditions
- Neoplasms, Clinical Documentation, Artificial Intelligence in Medicine
- Trial name
- NVC-AI-DOC (NCT07850700)
- Testing
- Ambient AI documentation system
- Where
- Lithuania
- Volunteers
- 250 people
- Sponsor
- National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos
End Stage Renal Disease
Impact of Clinical Pharmacy Services on Medication Cost and Hospitalization Rates in Hemodialysis Patients
The purpose of this study is to evaluate the effects of pharmaceutical care interventions in the ambulatory hemodialysis patients over a one-year period.
- Trial name
- NCT05952388
- Testing
- Behavioral Patient care
- Sponsor
- University of New Mexico